A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076137



Internal ID18972416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14313900..14314301hg38UCSC Ensembl
chr9:14313899..14314300hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769721
SamplesKWP1
Known GenesNFIB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076137
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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